JP2901815B2 - Method for producing polyester grain fabric - Google Patents
Method for producing polyester grain fabricInfo
- Publication number
- JP2901815B2 JP2901815B2 JP4185113A JP18511392A JP2901815B2 JP 2901815 B2 JP2901815 B2 JP 2901815B2 JP 4185113 A JP4185113 A JP 4185113A JP 18511392 A JP18511392 A JP 18511392A JP 2901815 B2 JP2901815 B2 JP 2901815B2
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- oil agent
- component
- weight
- polyester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 229920000728 polyester Polymers 0.000 title claims description 29
- 239000004744 fabric Substances 0.000 title claims description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 22
- 239000000835 fiber Substances 0.000 claims description 19
- 238000009941 weaving Methods 0.000 claims description 19
- 238000004513 sizing Methods 0.000 claims description 18
- -1 alcohol ester Chemical class 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 238000009835 boiling Methods 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 239000002759 woven fabric Substances 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 4
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 3
- 238000002074 melt spinning Methods 0.000 claims 1
- 239000003921 oil Substances 0.000 description 31
- 235000019198 oils Nutrition 0.000 description 31
- 238000009998 heat setting Methods 0.000 description 13
- 239000003292 glue Substances 0.000 description 11
- 235000014676 Phragmites communis Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000779 smoke Substances 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 4
- 239000004359 castor oil Substances 0.000 description 4
- 235000019438 castor oil Nutrition 0.000 description 4
- 238000002788 crimping Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 235000019484 Rapeseed oil Nutrition 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 230000002040 relaxant effect Effects 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000010025 steaming Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 208000016261 weight loss Diseases 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- VSEOZSAQQRETDU-UHFFFAOYSA-N 18-methylnonadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCC(C)C VSEOZSAQQRETDU-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241001589086 Bellapiscis medius Species 0.000 description 1
- MAEMSJLARDOJCZ-UHFFFAOYSA-N CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCCCCCCC(C)C Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCCCCCCC(C)C MAEMSJLARDOJCZ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVTJGGGYKAMDBN-UHFFFAOYSA-N Dioxetane Chemical compound C1COO1 BVTJGGGYKAMDBN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 244000273256 Phragmites communis Species 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000003490 Thiodipropionic acid Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- ITIHYXREPVHWNY-UHFFFAOYSA-N bis(16-methylheptadecyl) decanedioate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCCCCCCCCCC(C)C ITIHYXREPVHWNY-UHFFFAOYSA-N 0.000 description 1
- QZULIRBSQUIUTA-CLFAGFIQSA-N bis[(z)-octadec-9-enyl] hexanedioate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCC\C=C/CCCCCCCC QZULIRBSQUIUTA-CLFAGFIQSA-N 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 235000019303 thiodipropionic acid Nutrition 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Treatment Of Fiber Materials (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
- Woven Fabrics (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明はポリエステルシボ織物の
製造方法に関する。さらに詳しくは、製織時の製織性が
良好で且つシボ立て時にはシボ発現性の良好なポリエス
テルシボ織物の製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a polyester grain fabric. More specifically, the present invention relates to a method for producing a polyester crimped woven fabric which has a good weaving property at the time of weaving and a good crimping property at the time of crimping.
【0002】[0002]
【従来の技術】ポリエステルマルチフィラメントからシ
ボ織物を製造するには、該マルチフィラメントに約30
00回/mの強撚を付与した後、該強撚糸の製織性を高
めるために蒸熱処理して撚の旋回性を一時固定した後糊
付処理を行ない、次いで製織して得られる生機を熱水中
で緩和処理(以下RX処理と称することがある)して一
時的に固定した強撚糸の旋回性を再発現させると共に糊
剤を脱落させる方法が通常採用される。そして、この時
再発現される旋回性により、布帛に凹凸状のシボが発現
される。2. Description of the Related Art In order to produce a textured fabric from a polyester multifilament, the multifilament needs to have a thickness of about 30%.
After giving a strong twist of 00 turns / m, a steaming treatment is performed to temporarily fix the twisting property of the twist to enhance the weaving property of the strong twisted yarn, and then a sizing process is performed. In general, a method is used in which relaxation treatment (hereinafter sometimes referred to as RX treatment) in water is performed to re-exhibit the revolving property of the temporarily fixed strong twist yarn and to remove the paste. Then, due to the revolving property that is re-expressed at this time, an uneven grain is generated in the cloth.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、かかる
方法でポリエステルシボ織物を製造する場合、用いるポ
リエステル繊維の沸水収縮率が7〜9%以上である通常
のポリエステル繊維を用いると、RX処理時の強撚糸の
旋回性が低下すると共に残留トルクも弱くなって、シボ
立ち性が不充分となって風合が低下する。However, in the case of producing a polyester grain fabric by the above method, if a polyester fiber having a boiling water shrinkage of 7 to 9% or more is used, the strength during the RX treatment is reduced. The revolving property of the twisted yarn is reduced, and the residual torque is also weakened.
【0004】従来、ポリエステル繊維の沸水収縮率を低
下させる方法としては、熱セット温度を高める方法ある
いはリラックスさせながら熱セットを施す方法が知られ
ている。しかし、糊剤が付与されるポリエステル繊維の
場合、糊剤の剥離脱落を抑制するために鉱物油や一価エ
ステル化合物を主体成分とする油剤が付与されるが、耐
熱性に乏しいため高温での熱セットに適さないばかり
か、撚糸時に糸切れが多発しやすくなるという問題があ
る。かかる耐熱性を改善するために、ヤシ油やナタネ油
等の如き高分子量トリグリセライドを主体成分とする油
剤を付与すると、今度は製織工程で糊落ち等のスカムが
発生し易くなる。かかる糊落ちを解消する方法として
は、鉱物油を主成分とする油剤を熱セット後に付与する
方法も提案されているが、設備コスト、運転管理、さら
には油剤飛散による作業環境の点で好ましい方法とはい
い難い。Heretofore, as a method of reducing the boiling water shrinkage of polyester fibers, a method of increasing a heat setting temperature or a method of performing heat setting while relaxing is known. However, in the case of polyester fibers to which a sizing agent is applied, an oil agent containing a mineral oil or a monohydric ester compound as a main component is applied to suppress peeling and falling off of the sizing agent. Not only is it not suitable for heat setting, but also there is a problem that yarn breakage tends to occur frequently during twisting. When an oil agent such as coconut oil or rapeseed oil or the like having a high molecular weight as a main component such as coconut oil or rapeseed oil is applied in order to improve such heat resistance, scum such as glue drop easily occurs in the weaving process. As a method for eliminating such a size drop, a method of applying an oil agent containing a mineral oil as a main component after heat setting has also been proposed. However, this method is preferable in terms of equipment cost, operation management, and a work environment due to oil agent scattering. It is hard to say.
【0005】一方、リラックスさせながら熱セットする
方法は、延伸後に張力を緩和させながら繊維を走行させ
るため、張力調節用ローラーを設置する必要があり設備
コストが上昇するので好ましい方法とは言えない。[0005] On the other hand, the method of heat setting while relaxing is not a preferable method because the fiber is run while relaxing the tension after stretching, so that it is necessary to install a tension adjusting roller, which increases the equipment cost.
【0006】本発明は、上記従来技術を背景としてなさ
れたもので、その目的は、シボ立ち性の良好なポリエス
テルシボ織物を安価に製造する方法を提供することにあ
る。The present invention has been made on the background of the above-mentioned prior art, and an object of the present invention is to provide a method for inexpensively producing a polyester crimped fabric having good crimp standing.
【0007】[0007]
【課題を解決するための手段】本発明者らは、上記目的
を達成するために鋭意検討した結果、特定組成の油剤を
付与した後延伸熱セットしたポリエステル繊維は、製織
時の工程安定性は良好で、且つ強撚時の毛羽発生、製織
時の糊剤脱落が抑制されて、極めて良好なシボ織物が安
価に得られることを見出し本発明に到達した。Means for Solving the Problems The inventors of the present invention have conducted intensive studies to achieve the above object, and as a result, it has been found that a polyester fiber which is drawn and heat-set after an oil agent having a specific composition is applied has a stable process during weaving. The present invention was found to be able to obtain an excellent crimped woven fabric at a low cost, which is excellent and suppresses fluff generation during strong twisting and falling off of the paste during weaving.
【0008】すなわち、本発明によれば、ポリエステル
を溶融紡糸し、油剤を付与した後に沸水収縮率が5%以
下となるよう延伸熱セットしたポリエステル繊維に強撚
及び糊付けを施した糸条を製織し、しかる後該織物にシ
ボ立て処理を施すシボ織物の製造方法において、前記油
剤が下記(A)〜(C)を必須成分として含有し且つ
(I)〜(III )式を同時に満足することを特徴とする
ポリエステルシボ織物の製造方法、 (A)成分 常温で液状であって、分子量が550〜750の脂肪族
一価アルコールエステル (B)成分 次式で表わされる常温で液状の芳香族エステルThat is, according to the present invention, a polyester fiber is melt-spun, an oil agent is applied, and then a polyester fiber which is drawn and heat-set so as to have a boiling water shrinkage ratio of 5% or less is subjected to strong twisting and sizing, and is woven. Then, in the method for producing a textured fabric in which the fabric is subjected to a graining treatment, the oil agent contains the following (A) to (C) as essential components and simultaneously satisfies the formulas (I) to (III). (A) Component Aliphatic monohydric alcohol ester having a molecular weight of 550 to 750 and a liquid weight at room temperature (B) Component Aromatic ester liquid at room temperature represented by the following formula:
【0009】[0009]
【化2】 Embedded image
【0010】[但し、R1 ,R2 は炭素数8〜25のア
ルキル基、Aは炭素数2〜4のアルキレン基、n,mは
1又は2の整数を表わす。] (C)成分 常温で液状であって、分子内に水酸基を1個以上有する
トリグリセライドのアルキレンオキシド付加物 (I)WA +WB =20〜75 (II)WC =2〜15 (III )WA /WB =95/5〜60/40 [但し、WA ,WB 及びWC は、夫々(A)、(B)、
及び(C)成分の油剤有効成分に対する含有量(重量
%)を表わす。]が提供される。Wherein R 1 and R 2 represent an alkyl group having 8 to 25 carbon atoms, A represents an alkylene group having 2 to 4 carbon atoms, and n and m represent an integer of 1 or 2. (C) Component Alkylene oxide adduct of triglyceride which is liquid at normal temperature and has at least one hydroxyl group in the molecule. (I) W A + W B = 20 to 75 (II) W C = 2 to 15 (III) W A / W B = 95/5 to 60/40 [where W A , W B and W C are (A), (B),
And the content (% by weight) of the component (C) with respect to the oil agent active ingredient. ] Is provided.
【0011】本発明においては、優れたシボ立ち性、シ
ボ形態を発現させるためには旋回性の再発現を織物中で
最大限に発揮させる必要があり、そのためには、用いる
ポリエステル繊維の沸水収縮率を5%以下、好ましくは
3%以下にすることが重要な意義を有する。In the present invention, it is necessary to maximize the re-expression of the revolving property in the woven fabric in order to exhibit the excellent crimp standing and crimp morphology. It is important that the ratio be 5% or less, preferably 3% or less.
【0012】かかるポリエステル繊維を得るためには、
延伸後に170℃以上、好ましくは190℃以上の温度
で熱セットを行うことが肝要である。しかし一方では、
糊付け後製織するためには糊剤の脱落防止の観点から鉱
物油、低分子量の一価エステルを主体成分とする油剤を
付与することが好ましいとされているが、かかる油剤を
用いて170℃以上の高温で熱処理すると、発煙が多く
作業環境を著しく悪化させるとともにタールの発生が多
くなって得られる製品の品質が低下する。In order to obtain such a polyester fiber,
It is important to perform heat setting at a temperature of 170 ° C. or more, preferably 190 ° C. or more after stretching. But on the other hand,
In order to weave after gluing, it is said that it is preferable to apply a mineral oil and an oil agent having a low molecular weight monohydric ester as a main component from the viewpoint of preventing the adhesive agent from falling off. When the heat treatment is carried out at a high temperature, a large amount of smoke is generated and the working environment is remarkably deteriorated, and the amount of tar is increased to deteriorate the quality of the obtained product.
【0013】本発明者らは、シボ立ち性と糊剤の付着特
性、さらには強撚時の撚糸性及び製織時の工程特性等に
優れたポリエステル糸条について検討を重ねた結果、特
定成分を特定量含有する油剤を付与した後延伸熱セット
を行なったものが最適であるという知見を得た。The inventors of the present invention have repeatedly studied polyester yarns which are excellent in the crimping property and the adhesive properties of the sizing agent, the twisting property during strong twisting, and the processing properties during weaving. It has been found that the one obtained by applying a specific amount of the oil agent and then performing the stretching heat setting is optimal.
【0014】すなわち、本発明では前記(A)〜(C)
成分を必須成分として含有し、且つ(I)〜(III )式
を同時に満足する油剤を付与した後、沸水収縮率が5%
以下となるよう延伸熱セットすることが大切である。That is, in the present invention, the above (A) to (C)
After imparting an oil which contains the components as essential components and simultaneously satisfies the formulas (I) to (III), the boiling water shrinkage ratio is 5%.
It is important to set the stretching heat so as to be as follows.
【0015】まず脂肪族一価エステル(A)は、一価の
高級アルコールと、一価又は二価の脂肪族カルボン酸と
から得られるエステル化合物であって、その分子量は5
50〜750、好ましくは600〜700で、かつ常温
で液状を示す必要がある。具体的には、一価の高級アル
コールとして炭素数20〜34の高級アルコールを用
い、ステアリン酸、オレイン酸、パルミチン酸等の高級
脂肪酸又はアジピン酸、セバシン酸、チオジプロピオン
酸等の二塩基酸を用いた、モノ又はジエステル化合物を
あげることができ、イソエイコシルステアレート、イソ
ペンタコシルパルミテート、イソペンタコシルオレー
ト、イソペンタコシルエルシネート、等のモノエステ
ル、又はジイソステアリルチオジプロピオネート、ジオ
レイルアジペート、ジイソステアリルセバケート等のジ
エステルを例示することができる。First, the aliphatic monohydric ester (A) is an ester compound obtained from a monohydric higher alcohol and a monohydric or dihydric aliphatic carboxylic acid, and has a molecular weight of 5
It must be 50 to 750, preferably 600 to 700, and be liquid at room temperature. Specifically, higher alcohols having 20 to 34 carbon atoms are used as monohydric higher alcohols, and higher fatty acids such as stearic acid, oleic acid and palmitic acid or dibasic acids such as adipic acid, sebacic acid and thiodipropionic acid are used. And monoesters or diester compounds such as isoeicosyl stearate, isopentacosyl palmitate, isopentacosyl oleate, isopentacosyl erucinate, etc., and diisostearylthio. Diesters such as dipropionate, dioleyl adipate, diisostearyl sebacate and the like can be exemplified.
【0016】ここにおいて、分子量が750を越えるか
又は常温で固体状になる脂肪族一価アルコールエステ
ル、あるいはトリグリセライドであるヤシ油、ナタネ油
等の水酸基を有さない多価アルコールエステルのみをA
成分として用いた場合には、製織時の糊落ちが増大した
り、製糸時に走行糸と糸導との摩擦が増大して単糸切れ
が発生するようになり好ましくない。Here, only aliphatic monohydric alcohol esters having a molecular weight exceeding 750 or becoming solid at ordinary temperature, or polyhydric alcohol esters having no hydroxyl group such as coconut oil and rapeseed oil, which are triglycerides, are A
When used as a component, undesired increase in glue loss during weaving and increase in friction between the traveling yarn and the yarn guide during yarn production, resulting in the occurrence of single yarn breakage.
【0017】また、分子量が550未満の脂肪族一価ア
ルコールエステルでは、製糸時の熱により揮散し易くな
って発煙が生じ作業環境汚染の要因となるだけでなく、
熱ローラー、糸導等にタールを形成して単糸切れ等の要
因ともなり、また撚糸時の毛羽発生の要因ともなるため
好ましくない。In the case of an aliphatic monohydric alcohol ester having a molecular weight of less than 550, heat is liable to evaporate due to heat at the time of spinning, and smoke is generated, which not only causes pollution of the working environment,
It is not preferable because tar is formed on a heat roller, a yarn guide or the like, which may cause breakage of a single yarn, and may also cause fluffing during twisting.
【0018】次に芳香族エステル(B)は、下記一般式
で表わされる、ビスフェノールAにアルキレンオキサイ
ドを付加した後脂肪族モノカルボン酸でエステル化した
ジエステル化合物である。The aromatic ester (B) is a diester compound represented by the following general formula, which is obtained by adding an alkylene oxide to bisphenol A and then esterifying with an aliphatic monocarboxylic acid.
【0019】[0019]
【化3】 Embedded image
【0020】式中、R1 及びR2 は炭素数8〜25のア
ルキル基、Aは炭素数2〜4のアルキレン基、n、mは
1又は2の整数を表わす。R1 ,R2 の炭素数が8未満
の場合には、潤滑性が低下して耐擦過性が劣化し、原糸
毛羽や撚糸毛羽が増大する傾向にある。一方、炭素数が
25を越える場合には、工業的に入手し難いので好まし
くない。また、アルキレンオキサイドの付加モル数(n
又はm)が0の場合には、該芳香族エステルの性状が常
温で固状となるため、糊付け(サイジング)工程での糊
剤の付着性が阻害され、一方3以上の場合には親水性が
増加して糊皮膜を可塑化するため、せっかく糸上に形成
せしめた糊皮膜の保護作用が低減して製織効率が悪化す
るといった問題が生じる。In the formula, R 1 and R 2 represent an alkyl group having 8 to 25 carbon atoms, A represents an alkylene group having 2 to 4 carbon atoms, and n and m represent an integer of 1 or 2. When the number of carbon atoms of R 1 and R 2 is less than 8, lubricity is reduced, abrasion resistance is deteriorated, and fluff of the original yarn and fluff of the twisted yarn tend to increase. On the other hand, when the carbon number exceeds 25, it is not preferable because it is difficult to obtain industrially. In addition, the number of added moles of alkylene oxide (n
Or, when m) is 0, the properties of the aromatic ester become solid at room temperature, which impairs the adhesiveness of the sizing agent in the sizing step. Increases, and the glue film is plasticized, which causes a problem that the protective action of the glue film formed on the yarn is reduced and the weaving efficiency is deteriorated.
【0021】通常好ましく用いられる(B)成分として
は、例えばエチレンオキサイド2モル付加ビスフェノー
ルAのジラウレートをあげることができる。As the component (B) usually preferably used, there can be mentioned, for example, dilaurate of bisphenol A added with 2 moles of ethylene oxide.
【0022】本発明において用いられる油剤には、上記
に詳述した(A)成分と(B)成分との合計が、油剤有
効成分に対して20〜75重量%、好ましくは30〜6
5重量%含まれている必要がある。この含有量が20重
量%未満の場合には、製糸に要求される潤滑性を付与す
ることができず単糸切れの発生が増加する傾向にあり、
また製織時の“糊落ち”等の問題に対する改善効果も少
ない。一方、75重量%を越える場合には、油剤系の乳
化安定性に難点を生じるので好ましくない。In the oil agent used in the present invention, the sum of the components (A) and (B) described in detail above is 20 to 75% by weight, preferably 30 to 6% by weight, based on the active ingredient of the oil agent.
It must be contained at 5% by weight. If the content is less than 20% by weight, the lubricity required for yarn production cannot be provided, and the occurrence of single yarn breakage tends to increase,
In addition, there is little improvement effect on problems such as "glue removal" during weaving. On the other hand, if it exceeds 75% by weight, it is not preferable because it causes difficulty in the emulsion stability of the oil agent system.
【0023】また、本発明においては、(A)成分と
(B)成分との重量比(A/B)が95/5〜60/4
0の範囲内にあることが必要である。B成分の割合がA
とBの合計量に対して5重量%未満の場合には油剤の耐
熱性が低下し、逆に40重量%を越える場合には糸の摩
擦が高くなったり、後加工で糊付製織する際、糸上への
糊皮膜の接着性が低下したり、糊皮膜の凝集力を弱めて
サイジング効果を弱めてしまう結果となる。In the present invention, the weight ratio (A / B) between the component (A) and the component (B) is from 95/5 to 60/4.
Must be in the range of 0. The proportion of the B component is A
If the amount is less than 5% by weight with respect to the total amount of B and B, the heat resistance of the oil agent is reduced, and if it exceeds 40% by weight, the friction of the yarn increases, As a result, the adhesiveness of the glue film on the yarn is reduced, or the cohesive force of the glue film is weakened and the sizing effect is weakened.
【0024】本発明で用いられる油剤のもう一つの必須
成分である分子内に水酸基を有するトリグリセライドの
アルキレンオキシド付加物は、常温で液状であることが
必要である。また、その含有量は油剤の有効成分に対し
て2〜15重量%、好ましくは5〜10重量%含まれる必
要がある。The alkylene oxide adduct of triglyceride having a hydroxyl group in the molecule, which is another essential component of the oil agent used in the present invention, needs to be liquid at normal temperature. The content thereof must be 2 to 15% by weight, preferably 5 to 10% by weight, based on the active ingredient of the oil agent.
【0025】本発明は、かかるグリセライドのアルキレ
ンオキサイド付加物がポリエステルオリゴマー(主とし
て環状トリマー)との相溶性に優れ、ポリエステル繊維
製造時に加熱等の処理によって析出されるオリゴマーを
油剤系に溶解させるためと推定されるが、ローラー,糸
導ガイド等へのオリゴマースカム堆積を抑制する効果が
大きいことを見い出したものである。したがって、使用
量があまりに少なすぎるとこれらの効果が発現せず、一
方多すぎると前述A成分の効果(耐糊落ち性)を減ずる
とともに、走行糸と糸導との摩擦も増大して単糸摩擦が
増大したりするため好ましくない。The present invention is intended to dissolve such an oligomeric glyceride alkylene oxide adduct having excellent compatibility with a polyester oligomer (mainly a cyclic trimer) and to precipitate an oligomer precipitated by a treatment such as heating during the production of polyester fiber in an oil agent system. It is presumed that it has been found that the effect of suppressing the accumulation of oligomer scum on rollers, yarn guides, and the like is great. Therefore, if the amount is too small, these effects are not exhibited, while if it is too large, the effect of the above-mentioned component A (degreasing resistance) is reduced, and the friction between the running yarn and the yarn conductor is increased. It is not preferable because friction increases.
【0026】また、(C)成分において付加されている
アルキレンオキサイドは、炭素数が2〜4のアルキレン
オキサイドであって特にエチレンオキサイドが好まし
い。またその付加モル数は、水酸基を有するグリセライ
ドに対して4〜30モル、特に8〜15モルが望まし
い。付加モル数がこの範囲をはずれる場合にはポリエス
テルオリゴマーの溶解性が低下するためと推定される
が、オリゴマースカム堆積の抑制効果は低減する傾向が
ある。The alkylene oxide added in the component (C) is an alkylene oxide having 2 to 4 carbon atoms, and particularly preferably ethylene oxide. The number of moles to be added is preferably 4 to 30 mol, particularly preferably 8 to 15 mol, based on glyceride having a hydroxyl group. If the number of added moles is out of this range, it is presumed that the solubility of the polyester oligomer is reduced, but the effect of suppressing the accumulation of oligomer scum tends to be reduced.
【0027】かかるC成分としては、例えば硬化ヒマシ
油のアルキレンオキサイド付加物、及びこれらの脂肪族
モノカルボン酸モノエステル又はジエステルをあげるこ
とができる。具体的には、POE(8)硬化ヒマシ油エ
ーテル(POE(n)はオキシエチレンオキシドの付加
モル数が平均nモルであることを示す。以下同様)、P
OE(12)硬化ヒマシ油エーテル、POE(25)硬
化ヒマシ油ジラウレート等が好ましい。Examples of the component C include alkylene oxide adducts of hydrogenated castor oil and monoesters or diesters of these aliphatic monocarboxylic acids. Specifically, POE (8) hydrogenated castor oil ether (POE (n) indicates that the number of moles of oxyethylene oxide added is an average of n moles; the same applies hereinafter), P
Preferred are OE (12) hydrogenated castor oil ether, POE (25) hydrogenated castor oil dilaurate and the like.
【0028】なお、本発明の目的を損なわない範囲で他
の油剤成分を含有しても良いことはいうまでもない。か
かる配合剤としては、例えば、耐熱性を有するチオエス
テル系平滑剤、エマルジョンとして用いるための乳化
剤、静電気防止のための制電剤、耐熱性改善のための抗
酸化剤、さらには油剤の極圧潤滑性を高めたり油膜強度
を高めたりするための有機もしくは無機の添加剤等をあ
げることができる。It goes without saying that other oil components may be contained within a range not to impair the object of the present invention. Such compounding agents include, for example, thioester-based leveling agents having heat resistance, emulsifiers for use as emulsions, antistatic agents for preventing static electricity, antioxidants for improving heat resistance, and extreme pressure lubrication of oils. And organic or inorganic additives for enhancing the properties and the oil film strength.
【0029】かかる油剤をポリエステル繊維に付与する
には、紡出糸条が固化した時点以降であって延伸される
前であればよく、通常は引取りローラーより前の時点で
付与する。付与する好ましい手段としては、上述の油剤
を水系エマルジョンとなし、計量オイリングノズルを介
して付与する方法をあげることができるが、付与量は、
油剤純分として繊維重量に対して0.3〜1.0重量%
とすることが望ましく、かくすることにより得られる繊
維の製織効率等が一段と改善される。In order to apply such an oil agent to the polyester fiber, it is sufficient that the oil agent is applied after the spun yarn is solidified and before it is drawn. Usually, the oil agent is applied before the take-up roller. As a preferable means for applying, a method in which the above-mentioned oil agent is formed into an aqueous emulsion and applied via a metering oiling nozzle can be mentioned, but the applied amount is
0.3-1.0% by weight based on fiber weight as pure oil
It is preferable to improve the weaving efficiency and the like of the fiber obtained by the above.
【0030】本発明で用いられるポリエステル繊維は、
上記の油剤が付与された未延伸糸を沸水収縮率が5%以
下となるよう延伸熱セットして得る。例えば、図3に示
される如き装置を用いて1300m/分の速度で引き取
り、次いで引取りローラーと延伸熱セットローラーとの
間で3.0倍に延伸しながら170℃以上の温度で熱セ
ットすればよい。The polyester fibers used in the present invention are:
The undrawn yarn provided with the above oil agent is obtained by drawing heat setting so that the boiling water shrinkage is 5% or less. For example, the sheet is drawn at a speed of 1300 m / min using a device as shown in FIG. 3, and then heat set at a temperature of 170 ° C. or more while drawing 3.0 times between the drawing roller and a drawing heat setting roller. I just need.
【0031】かくの如くして製造されたポリエステル繊
維は、常法に従って撚係数K(撚数(回/m)×√(繊
度))=15000以上の強撚を施した後、糊付けして
製織され、しかる後得られた織物は例えば温度80〜1
00℃の熱水中に浸漬してシボ立てされる。The polyester fiber thus produced is subjected to strong twisting with a twist coefficient K (number of twists (times / m) × √ (fineness)) of 15,000 or more according to a conventional method, followed by pasting and weaving. The resulting fabric is then treated, for example, at a temperature of 80-1.
It is immersed in hot water at 00 ° C. and embossed.
【0032】[0032]
【発明の効果】以上に述べた本発明の方法によれば、従
来の方法からは得ることの難しかった熱水収縮率が5%
以下であり、且つ製糸時のスカム発生、撚糸時の毛羽発
生及び製織時の糊落ちが抑制されたポリエステル繊維が
得られ、シボ立ち性の良好なポリエステルシボ織物を簡
便に、且つ安価に製造することができ、その工業的価値
は極めて大きい。According to the method of the present invention as described above, the hot water shrinkage, which was difficult to obtain by the conventional method, is 5%.
It is possible to obtain a polyester fiber having the following characteristics, in which scum generation during spinning, fluff generation during twisting, and paste drop during weaving are suppressed, and a polyester crimp woven fabric having good crimp standing can be easily and inexpensively produced. And its industrial value is extremely large.
【0033】[0033]
【実施例】以下、本発明を実施例によりさらに詳述す
る。なお実施例において、シボ立ち性、耐熱性、ガイド
スカム、原糸毛羽、糊落ちスカムは夫々下記の方法によ
り評価した。EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples. In the examples, the crimping property, the heat resistance, the guide scum, the fluffiness of the raw yarn, and the scum removed from the paste were each evaluated by the following methods.
【0034】(1)耐熱性(耐発煙性、耐熱劣化性) ポリエステル繊維製造工程において、熱セット用加熱ロ
ーラーから発生する煙の状態、およびローラー周囲に発
生するタールの状況を目視し次の基準により判定した。 耐発煙性 ○ 発煙量少 △ 〃 中 × 〃 大 耐熱劣化性 ○ タール少 △ 〃 中 × 〃 大(1) Heat resistance (smoke resistance, heat deterioration resistance) In the polyester fiber manufacturing process, the state of smoke generated from the heat setting heating roller and the state of tar generated around the roller are visually observed and the following criteria. It was determined by Smoke resistance ○ Smoke generation small △ 〃 Medium × Large Heat deterioration resistance ○ Low tar △ 〃 Medium × 〃 Large
【0035】(2)ガイドスカム ポリエステル繊維製造工程において、熱セット用加熱ロ
ーラー通過後の糸ガイドに付着するスカム量を目視によ
り判定した。 ○ スカム少 △ 〃 中 × 〃 大(2) Guide scum In the polyester fiber production process, the amount of scum adhering to the yarn guide after passing through the heating roller for heat setting was visually determined. ○ Small scum △ 〃 Medium × 〃 Large
【0036】(3)原糸毛羽 原糸を160本採取して各20万m間の毛羽(単糸切
れ)の個数をカウントしこれから100万m当たりの毛
羽数を求め以下のように判定した。 毛羽個数(ケ/106 m) ○ 0〜0.5 △ 0.5〜2.0 × 2.0以上(3) Fuzzy yarns 160 yarns were collected, the number of fluffs (single yarn breaks) between each 200,000 m was counted, and the number of fluffs per 1 million m was obtained therefrom and judged as follows. . The number of fluff (ケ / 10 6 m) ○ 0 to 0.5 △ 0.5 to 2.0 × 2.0 or more
【0037】(4)撚糸毛羽 原糸に3000T/mの撚を付与した後、外観の毛羽を
目視により測定して下記の基準によって判定した。 外観毛羽(ケ/kg) ○ 0.5以下 △ 0.5〜1.0 × 1.0以上(4) Twisted nap After 3,000 T / m of twist was applied to the raw yarn, the appearance of the nap was visually measured and judged according to the following criteria. Appearance fluff (ke / kg) ○ 0.5 or less △ 0.5 to 1.0 × 1.0 or more
【0038】(5)糊落ちスカム 実際の製織工程での“糊落ち”現象に対する代用特性と
して、サイジング糸条の糸軸方向に作用する摩擦に対し
て、糸条表面の糊皮膜の一部が糸表面より剥離する剥離
頻度をもって評価した。(5) Paste scum As a substitute characteristic for the "paste bleeding" phenomenon in the actual weaving process, a part of the glue film on the surface of the yarn is affected by friction acting in the yarn axis direction of the sizing yarn. The evaluation was based on the frequency of peeling from the yarn surface.
【0039】ポリビニルアルコールとポリアクリル酸エ
ステルを主体とした糊剤で、目標付着量5.0重量%と
なるよう通常のローラーサイジング方法により、ポリエ
ステル繊維を糊付して、サイジング糸を得た。次に、こ
のサイジング糸20本を等間隔に配列し、両端が乱れな
いように固定端子を設置し、これを図1及び図2に示す
如く一端をチャック4によって固定し、多端に25g/
本の加重6を掛け、滑車5を通し試料全体に張力を与え
る。図に置いて1、2及び3は10cm間隔に設置された
筬であって可動台7に固定され、該可動台7は糸軸と平
行に5cm巾に亘って往復運動ができる。試料サイジング
糸は図2に示すように中央部筬2において108°の開
角度をもつように仕掛ける。A sizing yarn was obtained by sizing a polyester fiber with a sizing agent mainly composed of polyvinyl alcohol and polyacrylic acid ester by a usual roller sizing method so as to have a target adhesion amount of 5.0% by weight. Next, these 20 sizing yarns are arranged at equal intervals, fixed terminals are installed so that both ends are not disturbed, and one end is fixed by a chuck 4 as shown in FIGS.
A book weight 6 is applied and tension is applied to the entire sample through the pulley 5. In the figure, 1, 2 and 3 are reeds installed at 10 cm intervals, which are fixed to a movable table 7, and the movable table 7 can reciprocate in a width of 5 cm in parallel with the yarn axis. The sample sizing yarn is set so as to have an opening angle of 108 ° in the central reed 2 as shown in FIG.
【0040】次いで、可動台7を左右に往復運動させ、
10往復させた後に筬と糸条の擦過部分における糊皮膜
の剥離状態を注意深く観察し、剥離した試料本数の全試
料20本当りの割合をもって次のグレード付けで表わし
た。Next, the movable table 7 is reciprocated right and left,
After making 10 reciprocations, the peeling state of the adhesive film in the rubbed portion between the reed and the yarn was carefully observed, and the ratio of the number of peeled samples per 20 samples was expressed by the following grade.
【0041】なお、ここでは各3回の結果の平均をもっ
て判定した。 剥離本数割合 グレード 25%未満 : 良 25〜50% : 可 50%を越える: 不可 さらに実際に製織を行ない、糊落ちスカムを目視により
評価した結果をあわせて総合的に判断し糊落ちスカムと
して判定した。 糊落ちスカム ○ 少 △ 中 × 大Here, the determination was made based on the average of the results of each of the three times. Number of peeled pieces Grade Less than 25%: Good 25 to 50%: Acceptable Exceeding 50%: Impaired Further, weaving was performed, and the results of visual evaluation of the adhesive scum were comprehensively judged and judged as adhesive scum. did. Glue scum ○ Small △ Medium × Large
【0042】(6)シボ立ち リラックス処理後及び仕上り後のシボ立ちを目視により
判定した。 ◎ 極めて良好 ○ 良好 △ やや不十分 × 不可(6) Graining The graining after the relaxation treatment and after finishing was visually judged. ◎ Extremely good ○ Good △ Somewhat insufficient × Not possible
【0043】(7)残留トルク 撚糸後蒸熱処理により撚止めセットを行った糸条を、
1.2m切り取り中央に0.2g/dとなるように重り
をかけて両端を合わせる。糸条の有するトルクにより2
つ折りになった糸条に撚りが発生する。これを50cm切
り取り(糸の試長は1mある)検撚器により撚数を測定
しこれを2倍し、1m当りに直し残留トルクとする。(7) Residual torque The twist set after the twisting is performed by post-steaming heat treatment.
A 1.2-meter cutout is weighted at the center and 0.2 g / d, and both ends are combined. 2 depending on the torque of the yarn
Twist occurs in the folded yarn. This is cut off by 50 cm (the yarn has a test length of 1 m), the number of twists is measured by a twister, and the number is doubled.
【0044】 (8)沸水トルク 残留トルクと同様に撚止めセットを行った糸条を切り取
り、中央に0.2g/dとなるように重りをかけ両端を
合わせ、沸水中に1分間浸けた後、25cm切り取り(糸
の試長は50cmある)検撚器で撚数を測定しこれを4倍
し、1m当りに換算し沸水トルクとする。(8) Boiling Water Torque The twisted set yarn was cut out in the same manner as the residual torque, and the center was weighed at 0.2 g / d to adjust both ends, and immersed in boiling water for 1 minute. , 25 cm cut (yarn sample length is 50 cm) 4 times this measure the number of twists in the test twist device
It is converted to boiling water torque per meter.
【0045】(9)総合評価 下記の4段階で表わした。 ◎ 極めて良好 ○ 良好 △ やや不十分 × 不可(9) Overall evaluation The following four stages were used. ◎ Extremely good ○ Good △ Somewhat insufficient × Not possible
【0046】[0046]
【実施例1】固有粘度が0.65のポリエチレンテレフ
タレートを図3の装置を用いて溶融吐出して36フィラ
メントの糸条となした。この糸条をオイリングローラー
を介して表1に示した油剤を0.5重量%となるように
付与した。その後、引取ローラーにて1300m/分で
引取りながら90℃で予熱した後、引取ローラーと延伸
熱セットローラーとの間で3.0倍に延伸しながら13
0、150、170、190℃で熱セットし捲き取り7
5d/36f、強度4.6g/dの延伸糸を得た。Example 1 Polyethylene terephthalate having an intrinsic viscosity of 0.65 was melted and discharged using the apparatus shown in FIG. 3 to form a 36-filament yarn. This thread was applied via an oiling roller so that the oil agent shown in Table 1 was 0.5% by weight. Thereafter, the film was preheated at 90 ° C. while being taken up at 1300 m / min with a take-up roller, and then stretched 3.0 times between the take-up roller and a stretch heat set roller while being drawn 13 times.
Heat setting at 0, 150, 170, 190 ° C and winding up 7
A 5d / 36f drawn yarn having a strength of 4.6 g / d was obtained.
【0047】得られた延伸糸をイタリー撚糸機を用いて
3000T/mの撚を付与した後、85℃×30分のス
チーム熱処理を施して撚の一時固定を行なった。The obtained drawn yarn was twisted at 3000 T / m using an Italian twisting machine, and then subjected to steam heat treatment at 85 ° C. for 30 minutes to temporarily fix the twist.
【0048】該強撚糸を経糸用として引きそろえた後ア
クリル糸のサイジング剤を糸条重量に対して3.0%付
与し、一方サイジング剤を付与していない強撚糸を緯糸
として用い、経120本/25.4mm、緯84本/2
5.4mmの織密度で製織を行なった。得られた織物は、
液流染色機を用いて130℃×20分リラックス処理し
た後、水酸化ナトリウム35g/リットルのアルカリ水
溶液中100℃下減量率が18%となるよう減量処理を
行なった。次いで、分散染料を用い、130℃下45分
染色を行ない水洗後170℃で乾熱セットを行なった。After arranging the strong twisted yarn for warp, a sizing agent for the acrylic yarn was applied at 3.0% to the yarn weight, while a strong twisted yarn without the sizing agent was used as the weft. Book / 25.4mm, weft 84 book / 2
Weaving was performed at a weave density of 5.4 mm. The resulting fabric is
After a relaxation treatment at 130 ° C. for 20 minutes using a liquid dyeing machine, a weight reduction treatment was carried out in a 35 g / l aqueous solution of sodium hydroxide at 100 ° C. to a weight loss rate of 18%. Next, using a disperse dye, dyeing was performed at 130 ° C. for 45 minutes, and after washing with water, a dry heat setting was performed at 170 ° C.
【0049】得られたシボ織物の評価結果を表2に示
す。Table 2 shows the evaluation results of the obtained grain fabric.
【0050】[0050]
【表1】 [Table 1]
【0051】[0051]
【表2】 [Table 2]
【0052】上記結果より本発明の方法によれば、製糸
性、撚糸性、製織性、シボ立ち性共に極めて良好となる
ことがわかる。From the above results, it can be seen that, according to the method of the present invention, the spinning properties, the twisting properties, the weaving properties, and the creasing properties are all extremely good.
【0053】[0053]
【実施例2】実施例1と同様の装置を用い、表3記載の
油剤を付与した後延伸し190℃で熱セットを行なっ
て、シボ立ち性以外の項目について評価を行なった。結
果を表4に示す。Example 2 Using the same apparatus as in Example 1, the oils shown in Table 3 were applied, stretched, heat-set at 190 ° C., and items other than graining property were evaluated. Table 4 shows the results.
【0054】[0054]
【表3】 [Table 3]
【0055】[0055]
【表4】 [Table 4]
【0056】以上の結果から明らかなように、本発明に
かかる油剤を付与することによって、製糸、撚糸及び製
織工程が著しく改善されることがわかる。As is evident from the above results, it is understood that by applying the oil agent according to the present invention, the yarn-making, twisting and weaving steps are remarkably improved.
【図1】糊落ちスカム評価装置の側面図である。FIG. 1 is a side view of a glue removal scum evaluation device.
【図2】糊落ちスカム評価装置の平面図である。FIG. 2 is a plan view of the glue removal scum evaluation device.
【図3】実施例で使用したポリエステルの紡糸直延伸機
の略図である。FIG. 3 is a schematic view of a direct drawing machine for spinning polyester used in Examples.
1 糸条を擦過する筬 2 糸条を擦過する筬 3 糸条を擦過する筬 4 糸条固定用チェック 5 滑車 6 重り 7 筬を往復させる可動台 8 糸条 9 冷却装置 10 油剤付与装置 11 引取りローラー 12 延伸熱セットローラー 13 捲取機 DESCRIPTION OF SYMBOLS 1 Reed which rubs a thread 2 Reed which rubs a thread 3 Reed which rubs a thread 4 Thread fixing check 5 Pulley 6 Weight 7 Movable platform which reciprocates a reed 8 Thread 9 Cooling device 10 Oil supply device 11 Pull Take-up roller 12 Stretching heat set roller 13 Winding machine
フロントページの続き (56)参考文献 特開 昭52−25147(JP,A) 特開 昭56−37311(JP,A) 特開 昭62−149941(JP,A) 特開 昭55−163260(JP,A) 特開 昭58−220822(JP,A) 特開 昭55−93835(JP,A) 特公 昭62−45337(JP,B2) (58)調査した分野(Int.Cl.6,DB名) D06C 23/04 D01F 6/62 302 D03D 15/04 D06M 13/224 D06M 101:32 Continuation of the front page (56) References JP-A-52-25147 (JP, A) JP-A-56-37311 (JP, A) JP-A-62-149941 (JP, A) JP-A-55-163260 (JP, A) JP-A-58-220822 (JP, A) JP-A-55-93835 (JP, A) JP-B-62-45337 (JP, B2) (58) Fields investigated (Int. Cl. 6 , DB Name) D06C 23/04 D01F 6/62 302 D03D 15/04 D06M 13/224 D06M 101: 32
Claims (1)
した後に沸水収縮率が5%以下となるよう延伸熱セット
したポリエステル繊維に強撚及び糊付けを施した糸条を
製織し、しかる後該織物にシボ立て処理を施すシボ織物
の製造方法において、前記油剤が下記(A)〜(C)を
必須成分として含有し且つ(I)〜(III )式を同時に
満足することを特徴とするポリエステルシボ織物の製造
方法。 (A)成分 常温で液状であって、分子量が550〜750の脂肪族
一価アルコールエステル (B)成分 次式で表わされる常温で液状の芳香族エステル 【化1】 [但し、R1 ,R2 は炭素数8〜25のアルキル基、A
は炭素数2〜4のアルキレン基、n,mは1又は2の整
数を表わす。] (C)成分 常温で液状であって、分子内に水酸基を1個以上有する
トリグリセライドのアルキレンオキシド付加物 (I)WA +WB =20〜75 (II)WC =2〜15 (III )WA /WB =95/5〜60/40 [但し、WA ,WB 及びWC は、夫々(A)、(B)、
及び(C)成分の油剤有効成分に対する含有量(重量
%)を表わす。]Claims: 1. A polyester fiber obtained by melt-spinning a polyester, applying an oil agent thereto, and weaving a yarn obtained by subjecting a polyester fiber which has been drawn and heat-set to strong twisting and sizing so as to have a boiling water shrinkage ratio of 5% or less, and thereafter the woven fabric A method for producing a textured fabric, wherein the oil agent contains the following (A) to (C) as essential components and simultaneously satisfies the formulas (I) to (III). Fabrication method. (A) Component Aliphatic monohydric alcohol ester which is liquid at normal temperature and has a molecular weight of 550 to 750 (B) Component Aromatic ester which is liquid at normal temperature and represented by the following formula: [However, R 1 and R 2 are an alkyl group having 8 to 25 carbon atoms;
Represents an alkylene group having 2 to 4 carbon atoms, and n and m represent an integer of 1 or 2. (C) Component Alkylene oxide adduct of triglyceride which is liquid at normal temperature and has at least one hydroxyl group in the molecule. (I) W A + W B = 20 to 75 (II) W C = 2 to 15 (III) W A / W B = 95/5 to 60/40 [where W A , W B and W C are (A), (B),
And the content (% by weight) of the component (C) with respect to the oil agent active ingredient. ]
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4185113A JP2901815B2 (en) | 1992-07-13 | 1992-07-13 | Method for producing polyester grain fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4185113A JP2901815B2 (en) | 1992-07-13 | 1992-07-13 | Method for producing polyester grain fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0633365A JPH0633365A (en) | 1994-02-08 |
JP2901815B2 true JP2901815B2 (en) | 1999-06-07 |
Family
ID=16165093
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4185113A Expired - Fee Related JP2901815B2 (en) | 1992-07-13 | 1992-07-13 | Method for producing polyester grain fabric |
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Country | Link |
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JP (1) | JP2901815B2 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7062984B2 (en) * | 2018-02-06 | 2022-05-09 | 東レ株式会社 | Abrasion tester for the surface of raw yarn for woven fabrics |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6245337B2 (en) | 2016-11-01 | 2017-12-13 | サミー株式会社 | Pachinko machine |
-
1992
- 1992-07-13 JP JP4185113A patent/JP2901815B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6245337B2 (en) | 2016-11-01 | 2017-12-13 | サミー株式会社 | Pachinko machine |
Also Published As
Publication number | Publication date |
---|---|
JPH0633365A (en) | 1994-02-08 |
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